Atos Medical AB
Atos Medical AB holds FDA 510(k) medical device clearances, first cleared 1990, most recent 2016, with 1 FDA device recall on record.
Top product codes for Atos Medical AB
FDA recalls by Atos Medical AB
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Atos Medical AB
- K151404 — ProTrach Dualcare
- K141380 — PROVOX FREEHANDS FLEXIVOICE
- K131947 — PROVOX VEGA PUNCTURE SET
- K092593 — PROVOX ACTIVALVE (SIZE 4.5MM, 6MM, 8MM, 10MM, 12.5MM)
- K090455 — PROVOX VEGA, MODEL 8130-8135
- K072582 — PROVOX MICRON HME
- K043138 — PROVOX NID VOICE REHABILITATION SYSTEM, MODEL REF 7101 TO 7134
- K022125 — PROVOX FREEHANDS HME, MODEL 7710
- K014102 — PROVOX HME CASSETTE, MODEL 7240; PROVOX ADHESIVE, MODEL 7251
- K971244 — PROVOX 2 VOICE PROSTHESIS SYSTEM
- K942495 — SINOJET MAXILLARY SINUS PUNCTURE & IRRIGATION SYSTEM
- K940638 — PROVOX(TM) VOICE PROSTHESIS
- K936275 — TYMPOVENT
- K922145 — SINOJECT MAXILLARY SINUS PUNCTURE & IRRIGATION SYS
- K896630 — SINOVENT MAXILLARY SINUS DRAINAGE SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.